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1.
Whole exome sequencing and polygenic assessment of a Swedish cohort with severe developmental language disorder.
Hum Genet
; 143(2): 169-183, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38300321
2.
Circular RNAs arising from synaptic host genes during human neuronal differentiation are modulated by SFPQ RNA-binding protein.
BMC Biol
; 21(1): 127, 2023 05 26.
Article
in English
| MEDLINE | ID: mdl-37237280
3.
Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium.
Mol Psychiatry
; 27(4): 2114-2125, 2022 04.
Article
in English
| MEDLINE | ID: mdl-35136228
4.
Preferential looking to eyes versus mouth in early infancy: heritability and link to concurrent and later development.
J Child Psychol Psychiatry
; 64(2): 311-319, 2023 02.
Article
in English
| MEDLINE | ID: mdl-36426800
5.
Infants' sense of approximate numerosity: Heritability and link to other concurrent traits.
Dev Sci
; 26(4): e13347, 2023 07.
Article
in English
| MEDLINE | ID: mdl-36395061
6.
In search of environmental risk factors for obsessive-compulsive disorder: study protocol for the OCDTWIN project.
BMC Psychiatry
; 23(1): 442, 2023 06 16.
Article
in English
| MEDLINE | ID: mdl-37328750
7.
Modeling SHH-driven medulloblastoma with patient iPS cell-derived neural stem cells.
Proc Natl Acad Sci U S A
; 117(33): 20127-20138, 2020 08 18.
Article
in English
| MEDLINE | ID: mdl-32747535
8.
Pupil size and pupillary light reflex in early infancy: heritability and link to genetic liability to schizophrenia.
J Child Psychol Psychiatry
; 63(9): 1068-1077, 2022 09.
Article
in English
| MEDLINE | ID: mdl-34939671
9.
Determining Zygosity in Infant Twins - Revisiting the Questionnaire Approach.
Twin Res Hum Genet
; 24(3): 168-175, 2021 06.
Article
in English
| MEDLINE | ID: mdl-34247691
10.
The Babytwins Study Sweden (BATSS): A Multi-Method Infant Twin Study of Genetic and Environmental Factors Influencing Infant Brain and Behavioral Development.
Twin Res Hum Genet
; 24(4): 217-227, 2021 08.
Article
in English
| MEDLINE | ID: mdl-34521499
11.
The Association Between Somatic Health, Autism Spectrum Disorder, and Autistic Traits.
Behav Genet
; 50(4): 233-246, 2020 07.
Article
in English
| MEDLINE | ID: mdl-31811521
12.
Clinical versus automated assessments of morphological variants in twins with and without neurodevelopmental disorders.
Am J Med Genet A
; 182(5): 1177-1189, 2020 05.
Article
in English
| MEDLINE | ID: mdl-32162839
13.
Long-term social skills group training for children and adolescents with autism spectrum disorder: a randomized controlled trial.
Eur Child Adolesc Psychiatry
; 28(2): 189-201, 2019 Feb.
Article
in English
| MEDLINE | ID: mdl-29748736
14.
Copy number variation and neuropsychiatric problems in females and males in the general population.
Am J Med Genet B Neuropsychiatr Genet
; 180(6): 341-350, 2019 09.
Article
in English
| MEDLINE | ID: mdl-30307693
15.
Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes.
BMC Genomics
; 19(1): 432, 2018 Jun 04.
Article
in English
| MEDLINE | ID: mdl-29866042
16.
Copy Number Variation Analysis of 100 Twin Pairs Enriched for Neurodevelopmental Disorders.
Twin Res Hum Genet
; 21(1): 1-11, 2018 02.
Article
in English
| MEDLINE | ID: mdl-29307321
17.
Ciliary dyslexia candidate genes DYX1C1 and DCDC2 are regulated by Regulatory Factor X (RFX) transcription factors through X-box promoter motifs.
FASEB J
; 30(10): 3578-3587, 2016 10.
Article
in English
| MEDLINE | ID: mdl-27451412
18.
A Novel Way to Measure and Predict Development: A Heuristic Approach to Facilitate the Early Detection of Neurodevelopmental Disorders.
Curr Neurol Neurosci Rep
; 17(5): 43, 2017 May.
Article
in English
| MEDLINE | ID: mdl-28390033
19.
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes.
Hum Mol Genet
; 23(10): 2752-68, 2014 May 15.
Article
in English
| MEDLINE | ID: mdl-24381304
20.
Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes.
Hum Genet
; 134(2): 191-201, 2015 Feb.
Article
in English
| MEDLINE | ID: mdl-25432440